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Internship Downstream Process Development Scientist information

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How much do internship downstream process development scientist jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for internship downstream process development scientist in Ridgefield, CT is $38.51, according to ZipRecruiter salary data. Most workers in this role earn between $28.27 and $45.96 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Internship Downstream Process Development Scientist, and why are they important?

To thrive as an Internship Downstream Process Development Scientist, you need foundational knowledge in biochemistry, molecular biology, or chemical engineering, often supported by ongoing or recent enrollment in a relevant degree program. Familiarity with laboratory techniques such as chromatography, filtration, and analytical instruments, as well as experience with lab management software, is typically expected. Attention to detail, problem-solving abilities, and effective teamwork are standout soft skills in this role. These skills and qualifications are crucial for conducting reliable experiments, analyzing data, and contributing to the optimization of bioprocesses in a collaborative research environment.

What does an Internship Downstream Process Development Scientist do?

An Internship Downstream Process Development Scientist works in the biopharmaceutical industry, assisting with the development and optimization of processes that purify biological products such as proteins, antibodies, or vaccines after they are produced by cells. Their role often involves supporting laboratory experiments, analyzing samples, and documenting results to improve the efficiency and scalability of downstream processes like filtration and chromatography. Interns in this position gain hands-on experience with cutting-edge technologies and learn about regulatory requirements and industry standards. This role helps prepare students or recent graduates for a career in process development or biomanufacturing.

What types of projects and responsibilities can an Internship Downstream Process Development Scientist expect to work on?

As an Internship Downstream Process Development Scientist, you can expect to be involved in hands-on laboratory work focusing on the purification and characterization of biopharmaceutical products. Typical responsibilities include preparing buffer solutions, operating chromatography and filtration systems, analyzing samples using various analytical techniques, and documenting experimental results. Interns often collaborate with experienced scientists and engineers, contributing to process optimization and troubleshooting. The role provides valuable exposure to industry-standard procedures and the opportunity to develop technical skills in a team-oriented environment.
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Director, Formulation and Process Development

Director, Formulation and Process Development

AstraZeneca

New Haven, CT • On-site

$175K - $263K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 12 days ago

AstraZeneca rating

8.6

Company rating: 8.6 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

16th of 71 rated pharmaceutical

Job description

You will lead and direct the formulation and process development of patient-centered injectable drug products. These products are for Alexion's diverse portfolio, which spans synthetic, peptide, genomic medicine, and protein-based modalities in multiple formats, including liquid, lyophilized, vial, prefilled, and cartridge-based presentations. You will also lead life cycle development opportunities, provide expertise in technology transfer and drug product engineering and technology development with internal and external partnerships. You will also ensure the development of portfolio projects in a phase-appropriate manner while managing the budget and interface partners. You will be a member of the Injectable Drug Product Management team and will need to collaborate and network with other departments within Product Development and Clinical Supplies (PDCS). Additionally, it will need to collaborate and network with Alexion Operations, Clinical Development, Quality, and Regulatory organizations.
You Will:
  • Formulation and process development and manufacturing of patient-centered, unique injectable drug products for Alexion's diverse portfolio from pre-clinical to successful licensure.

  • Develop drug product development strategies through internal/external partnerships and product integration into drug/device combination products.

  • Enable the progression of Alexion's diverse portfolio that spans peptide, nucleic acid, protein-based modalities, as well as modalities for gene delivery as liquid and lyophilized dosage forms in vial, prefilled syringe, and cartridge-based presentations.

  • Ensure tech transfer of Alexion's portfolio with specialized input on engineering solutions for equipment and processes.

  • Review and develop drug product technology roadmap and manage important investments.

  • Mentor and develop colleagues in a matrix team for efficient and successful drug product development and manufacturing in a phase appropriate manner.

  • Partner with functions across Alexion to build the best strategies for developing products in Alexion's diverse portfolio.

  • Provide subject matter expertise for preparing regulatory filings, regulatory interactions including inspections, audits and is accountable for the technical content of the relevant drug product sections of regulatory submissions.

  • Work with the Head on the development on drug product development strategies within PDCS and with partners in Operations, Regulatory Affairs, and Commercial organizations.

You Have:
  • Must have a BS or equivalent in Bio/Chemical Engineering, Pharmaceutical Sciences, Biochemistry, or related discipline with relevant experience

  • At least 8 years of experience in managing a group of drug product development scientists or engineers with end to end drug product development experience (spanning formulation, process development, quality attribute assessment, tech transfer and manufacturing support) for mAbs, fusion proteins, injectable peptides/synthetics programs.

  • At least 5 years of experience managing a team of scientists and engineers at different levels (directly or in a matrix team) and ensuring their career growth.

  • Must be proficient in current approaches for formulation and drug product process development, manufacturing processes and equipment, regulatory expectations and applying these to developing efficient approaches to ensure product licensure.

  • Knowledge of high concentration protein formulation development, aseptic processes, vial, prefilled syringe, cartridge presentations, liquid and lyophilization dosage forms is important.

  • Knowledge of current regulatory guidelines and cGMP requirements is necessary

Benefits offered include:
  • A qualified retirement program [401(k) plan]

  • Paid vacation, holidays, and paid leaves

  • Health benefits including medical, prescription drug, dental, and vision coverage following the terms and conditions of the applicable plans.

Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. The annual base salary for this position ranges from $175,000 to $263,000. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles).
#LI-Onsite #Alexion
Date Posted
29-May-2026
Closing Date
29-Jun-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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